TY - JOUR
T1 - Genetic and epigenetic determinants of DNA replication origins, position and activation
AU - Méchali, Marcel
AU - Yoshida, Kazumasa
AU - Coulombe, Philippe
AU - Pasero, Philippe
N1 - Funding Information:
We thank members of the Méchali and Pasero laboratories for discussion and comments. Work in the Méchali laboratory is supported by the European Research Council (ERC) under the European Community's Seventh Framework Programme ( FP7/2007-201 ), by the ‘Agence Nationale de la Recherche’ (ANR) , the ARC , the ‘Ligue Nationale Contre le Cancer’ (LNCC) , and by the ‘Fondation pour la Recherche Médicale’ (FRM) . Work in the Pasero laboratory is supported by the ‘Agence Nationale pour la Recherche’ (ANR), the ‘Institut National du Cancer’ (INCa) and the ‘Ligue contre le Cancer (équipe labellisée)’. KY is a fellow of the ‘Ligue contre le Cancer’. PC was supported by the FRM and ARC. We apologize to those whose work has not been cited because of space constraints.
PY - 2013/4
Y1 - 2013/4
N2 - In the genome of eukaryotic cells, DNA synthesis is initiated at multiple sites called origins of DNA replication. Origins must fire only once per cell cycle and how this is achieved is now well understood. However, little is known about the mechanisms that determine when and where replication initiates in a given cell. A large body of evidence indicates that origins are not equal in terms of efficiency and timing of activation. Origin usage also changes concomitantly with the different cell differentiation programs. As DNA replication occurs in the context of chromatin, initiation could be influenced by multiple parameters, such as nucleosome positioning, histone modifications, and three-dimensional (3D) organization of the nucleus. This view is supported by recent genome-wide studies showing that DNA replication profiles are shaped by genetic and epigenetic processes that act both at the local and global levels to regulate origin function in eukaryotic cells.
AB - In the genome of eukaryotic cells, DNA synthesis is initiated at multiple sites called origins of DNA replication. Origins must fire only once per cell cycle and how this is achieved is now well understood. However, little is known about the mechanisms that determine when and where replication initiates in a given cell. A large body of evidence indicates that origins are not equal in terms of efficiency and timing of activation. Origin usage also changes concomitantly with the different cell differentiation programs. As DNA replication occurs in the context of chromatin, initiation could be influenced by multiple parameters, such as nucleosome positioning, histone modifications, and three-dimensional (3D) organization of the nucleus. This view is supported by recent genome-wide studies showing that DNA replication profiles are shaped by genetic and epigenetic processes that act both at the local and global levels to regulate origin function in eukaryotic cells.
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U2 - 10.1016/j.gde.2013.02.010
DO - 10.1016/j.gde.2013.02.010
M3 - Review article
C2 - 23541525
AN - SCOPUS:84877815977
SN - 0959-437X
VL - 23
SP - 124
EP - 131
JO - Current Opinion in Genetics and Development
JF - Current Opinion in Genetics and Development
IS - 2
ER -